Piperidines

<p>Stability Volatile<br>Applications In the presence of sugars, lysine, similarly to asparagine and phenylalanine, can undergo carbonyl-assisted decarboxylative deamination reaction to generate pent-4-en-1-amine, the counterpart of acrylamide.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Stadler, R., et al.: Chem. Res. Toxicol., 16, 1242 (2003), Stadler, R., et al.: J. Agric. Food Chem., 52, 5550 (2004),<br></p>

<p>Applications 4-(2-Aminoethyl)tetrahydropyran is a useful pharmaceutical intermediate.<br>References Prime, M. E., et al.: ACS Med. Chem. Lett., 3, 731 (2012); Ho, G. D., et al.: Bioorg. Med. Chem. Lett., 22, 1019 (2012)<br></p>

<p>Applications N-Benzyl-3-hydroxypiperidine has been used as a reactant in the preparation of optically active azidopiperidines.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Cochi, A., et. al.: Eur. J. Org. Chem., 2012, 2023 (2012)<br></p>

<p>Applications 4-Benzyl-4-piperidinol, is a building block used for the synthesis of various compounds, having therapeutic properties, such as synthesis of 4-Benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.<br>References Ting, P. C., et al.: Bioorg. Med. Chem. Lett., 20, 5004 (2010);<br></p>